Abstract:Two antibiotics have been isolated from a strain of Rhodococcus fascians that emerged from a competitive co-culture with Streptomyces padanus. The structures of these compounds were elucidated by detailed analyses by NMR and MS. They belong to the aminoglycoside family of antibiotics, and they are structurally unrelated to the actinomycins that are produced by S. padanus. The compounds have been named rhodostreptomycins A and B, reflecting their rhodococcal origin and streptomycin-like composition. Rhodostrept… Show more
“…The horizontal exchange of genes in these pathways is well documented (18,21,23,26) and provides a rapid mechanism for bacteria to test the selective advantage afforded by the small molecule product(s) of complex biosynthetic pathways (12,23). Documenting the distributions of specific biosynthetic pathways among bacteria has the potential to add new insight into the extent to which these pathways are exchanged and how gene clusters evolve to create new chemical diversity.…”
The marine actinomycete genus Salinispora is composed of three closely related species. These bacteria are a rich source of secondary metabolites, which are produced in species-specific patterns. This study examines the distribution and phylogenetic relationships of genes involved in the biosynthesis of secondary metabolites in the salinosporamide and staurosporine classes, which have been reported for S. tropica and S. arenicola, respectively. The focus is on "Salinispora pacifica," the most recently discovered and phylogenetically diverse member of the genus. Of 61 S. pacifica strains examined, 15 tested positive for a ketosynthase (KS) domain linked to the biosynthesis of salinosporamide K, a new compound in the salinosporamide series. Compound production was confirmed in two strains, and the domain phylogeny supports vertical inheritance from a common ancestor shared with S. tropica, which produces related compounds in the salinosporamide series. There was no evidence for interspecies recombination among salA KS sequences, providing further support for the geographic isolation of these two salinosporamide-producing lineages. In addition, staurosporine production is reported for the first time for S. pacifica, with 24 of 61 strains testing positive for staD, a key gene involved in the biosynthesis of this compound. High levels of recombination were observed between staD alleles in S. pacifica and the cooccurring yet more distantly related S. arenicola, which produces a similar series of staurosporines. The distributions and phylogenies of the biosynthetic genes examined provide insight into the complex processes driving the evolution of secondary metabolism among closely related bacterial species.
“…The horizontal exchange of genes in these pathways is well documented (18,21,23,26) and provides a rapid mechanism for bacteria to test the selective advantage afforded by the small molecule product(s) of complex biosynthetic pathways (12,23). Documenting the distributions of specific biosynthetic pathways among bacteria has the potential to add new insight into the extent to which these pathways are exchanged and how gene clusters evolve to create new chemical diversity.…”
The marine actinomycete genus Salinispora is composed of three closely related species. These bacteria are a rich source of secondary metabolites, which are produced in species-specific patterns. This study examines the distribution and phylogenetic relationships of genes involved in the biosynthesis of secondary metabolites in the salinosporamide and staurosporine classes, which have been reported for S. tropica and S. arenicola, respectively. The focus is on "Salinispora pacifica," the most recently discovered and phylogenetically diverse member of the genus. Of 61 S. pacifica strains examined, 15 tested positive for a ketosynthase (KS) domain linked to the biosynthesis of salinosporamide K, a new compound in the salinosporamide series. Compound production was confirmed in two strains, and the domain phylogeny supports vertical inheritance from a common ancestor shared with S. tropica, which produces related compounds in the salinosporamide series. There was no evidence for interspecies recombination among salA KS sequences, providing further support for the geographic isolation of these two salinosporamide-producing lineages. In addition, staurosporine production is reported for the first time for S. pacifica, with 24 of 61 strains testing positive for staD, a key gene involved in the biosynthesis of this compound. High levels of recombination were observed between staD alleles in S. pacifica and the cooccurring yet more distantly related S. arenicola, which produces a similar series of staurosporines. The distributions and phylogenies of the biosynthetic genes examined provide insight into the complex processes driving the evolution of secondary metabolism among closely related bacterial species.
“…Recently, a new methodology was intruduced via coculture between a strain of Rhodococcus fascians that does not produce an antibiotic and a strain of S. padanus that is a highly stable actinomycin producer [7]. The Rhodococcus strain 307CO isolated from one such coculture produced novel antibiotics (rhodostreptomycin A and rhodostreptomycin B), which are isomers different from the configuration of the carbon atom at C6 in streptose [7].…”
Section: Introductionmentioning
confidence: 99%
“…Recently, a new methodology was intruduced via coculture between a strain of Rhodococcus fascians that does not produce an antibiotic and a strain of S. padanus that is a highly stable actinomycin producer [7]. The Rhodococcus strain 307CO isolated from one such coculture produced novel antibiotics (rhodostreptomycin A and rhodostreptomycin B), which are isomers different from the configuration of the carbon atom at C6 in streptose [7]. Genetic analysis showed that a strain of Rhodococcus strain 307CO contained a large segment DNA derived from the Streptomyces strains, and there is correlation between antibiotic production and the presence of the Streptomyces DNA in the Rhodococcus [7].…”
In order to produce a new antibiotic material against Jurkat T cells using horizontal gene transfer among microbes, co-cultures between soil bacteria AY2000 and the multiple antibiotic producer S. griseus was carried out. It showed that the highest active substance against Jurkat T cells was produced at 48 hr of co-culture time with MTT assay. Moreover, a morphological change of nuclear of Jurkat T cells treated with co-cultured substance was observed in DAPI staining. This result suggests that a new material was produced with co-culture supernatant, and that co-culture between microboes can develop new antibiotic materials.
“…Em estudos prévios, a utilização de culturas mistas estimulou a produção de metabólitos secundários e/ou aumentou a atividade biológica de extratos microbianos (WHITT et al, 2014;CHAGAS;DIAS;PUPO, 2013, RATEB et al, 2013ONAKA et al, 2011;NEWMAN, 2011;GLAUSER et al, 2009;PARK et al, 2009;PETTIT, 2009;KUROSAWA et al, 2008;ZHU et al, 2007;ANGELL et al, 2006;LIN, 2006;OH et al, 2005;DEGENKOLB et al, 2002;CUETO et al, 2001;SLATTERY;RAJBHANDARI;WESSON, 2001 A biossíntese do antibiótico pestalona (Figura 3) pelo fungo Pestalotia sp., é um exemplo de indução da expressão de uma rota biossintética em resposta a co-cultura com bactéria marinha unicelular (CUETO et al, 2001). Os diterpenos libertelenona A-D (Figura 3) também foram produzidos em resposta às interações microbianas na co-cultura entre o fungo Libertella sp.…”
Section: Interações Microbianas E Culturas Mistasunclassified
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